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  • Wiley-Blackwell  (2,434)
  • PANGAEA
  • 1975-1979  (2,389)
  • 1935-1939  (103)
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  • 1
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    Unknown
    PANGAEA
    In:  Supplement to: White, Stan; Warnke, Detlef A; Nilsen, T H; Müller, Carla; Morris, D A; Kharin, Gennady S; Faas, Richard W; Caston, V S D; Bjorklund, Kjell R; Talwani, Manik; Udintsev, Gleb B (1976): Initial Reports of the Deep Sea Drilling Project. Initial Reports of the Deep Sea Drilling Project, U.S. Government Printing Office, XXXVIII, 1256 pp, https://doi.org/10.2973/dsdp.proc.38.1976
    Publication Date: 2023-08-28
    Description: Because of its position between the North Atlantic and the Arctic oceans, its young age, small size, and diversity of geological structures, the Norwegian-Greenland Sea provided a unique target for deep drilling on Leg 38 of the Glomar Challenger. From studies of the sediments and basement rocks it was expected to gain insight particularly as to the following: 1) The tectonic framework and evolution of this area with special emphasis on the continental margins and on questions concerned with shifts of spreading axis and existence of foundered continental areas. 2) The youngest times of existence of land bridges between Eurasia and North America and the effect these land bridges had on water circulation and paleoclimates. 3) The date of the initiation of glaciation and dates of glacial advances and retreats. 4) Description of the Tertiary marine microfauna and microflora of the Norwegian-Greenland Sea, which are essentially unknown at present, and investigation of their similarity with microfauna and microflora from other areas.
    Keywords: 38-337; 38-345; 38-347; 38-349; Comment; Deep Sea Drilling Project; Deposit type; DEPTH, sediment/rock; Description; DRILL; Drilling/drill rig; DSDP; Event label; Glomar Challenger; Identification; Leg38; NOAA and MMS Marine Minerals Geochemical Database; NOAA-MMS; North Atlantic/Norwegian Sea/BASIN; North Atlantic/Norwegian Sea/RIDGE; Position; Quantity of deposit; Sample code/label; Sediment type; Substrate type; Visual description
    Type: Dataset
    Format: text/tab-separated-values, 81 data points
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  • 2
    facet.materialart.
    Unknown
    PANGAEA
    In:  Supplement to: Montadert, Lucien; Roberts, David G; Auffret, Gérard A; Bock, W D; Dupeuble, P A; Hailwood, Ernie A; Harrison, William E; Kagami, H; Lumsden, D N; Müller, C M; Schnitker, Detmar; Thompson, T L; Timofeev, Pyotr P (1979): Initial Reports of the Deep Sea Drilling Project. U. S. Government Printing Office, XLVIII, 1183 pp, https://doi.org/10.2973/dsdp.proc.48.1979
    Publication Date: 2023-08-28
    Description: Unlike many cruises of the Deep Sea Drilling Project, Leg 48 was scientifically planned to drill a number of sites to systematically address the problems of passive margin evolution. Site 400 was drilled at the foot of the Meriadzek Escarpment of North Biscay in 4399 meters depth. The site was located in a half-graben forming part of a succession of tilted and rotated fault blocks near the continent/ocean boundary. Site 401 was situated on the planated edge of a tilted fault-block underlying the southern edge of the Meriadzek Terrace on the north Biscay margin. Site 402 was located on the upper slope of the northern continental margin of the Bay of Biscay. The main objectives were to establish the presence or absence of shallow water Upper Cretaceous beds, and to penetrate pre-Aptian synrift sediments and the upslope equivalent of the deep water Albian-Aptian carbonaceous mudstones penetrated at Hole 400A.
    Keywords: 48-400A; 48-401; 48-402; Comment; Deep Sea Drilling Project; Deposit type; DEPTH, sediment/rock; Description; DRILL; Drilling/drill rig; DSDP; Event label; Glomar Challenger; Identification; Leg48; NOAA and MMS Marine Minerals Geochemical Database; NOAA-MMS; North Atlantic/BASIN; North Atlantic/SLOPE; North Atlantic/TERRACE; Position; Quantity of deposit; Sample code/label; Sediment type; Substrate type; Visual description
    Type: Dataset
    Format: text/tab-separated-values, 67 data points
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Biotechnology and Bioengineering 17 (1975), S. 1679-1693 
    ISSN: 0006-3592
    Keywords: Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: The suitability of hornblende as a support for immobilized β-fructofuranosidase (invertase) was studied, with regard to the physical stability of the support and the thermal and operational stability of the immobilized enzyme. Hornblende was more stable than Enzacryl-Alo or Enzacryl-TIO, and marginally more stable than porous glass. Invertase immobilized on hornblende was more stable during long-term operation than invertase immobilized on porous glass. An active preparation of immobilized invertase was obtained also on pyroxene particles.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 15 (1977), S. 973-981 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Linear D2-m-carborane-siloxanes with one, two, and three trifluoropropyl moieties per repeat unit were prepared by the condensation reaction between bisureidosilanes and carborane disilanol. Molecular weights between 100,000 and 220,000 were obtained. Compared to fluorosilicones, the trifluoropropyl-modified carborane-siloxanes exhibited greater thermal and oxidative stability and in certain cases comparable solvent resistance. The swelling index for carborane-siloxane elastomers decreased with increasing trifluoropropyl content, although this fluorocarbon moiety did compromise the thermal stability of the carborane system.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 17 (1979), S. 1153-1161 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: To elucidate mechanisms in electroinitiated polymerization reactions a comparison was conducted between ultraviolet (UV) photoinitiation and electroinitiation of N-vinyl phthalimide with zinc chloride as a catalyst. Both methods give low yields of a complex polymer product. A detailed analysis, infrared (IR), gel permeation chromatography (GPC), elemental, and molecular weight, conducted on the polymeric products, indicated that phthalimide ring opening was occurring and that complex mixtures of poly(N-vinyl phthalimide) derivatives were formed. Both initiation methods gave comparable results, which further indicated mechanistic similarity between photo-and electroinitiation in these donor-acceptor charge transfer polymerizations.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Letters Edition 15 (1977), S. 399-405 
    ISSN: 0360-6384
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 15 (1977), S. 1563-1571 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: As part of a program to extend the range of donor-acceptor-initiated polymerization processes, the electroinitiation of 2-vinylnaphthalene in a zinc chloride-sulfolane solution has been studied. Good conversion yields of well-characterized (NMR, IR, GPC, elemental analysis) poly(vinylnaphthalene) were obtained with the process showing several mechanistic similarities to other donor-acceptor salt electropolymerization systems.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 15 (1977), S. 1555-1562 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The electrochemically initiated polymerization of styrene in methylene chloride solvent with the use of platinum electrodes and tetraalkyl and -aryl group VA halides (i.e., quaternary ammonium, phosphonium, and arsonium compounds) as electrolyte has been investigated. The order of reactivity of the electrolytes with respect to polymerization rate and initiation efficiency was found to be: arsonium 〉 phosphonium 〉 ammonium. Mechanisms involving the electroreduction of the group VA quaternary halides to species capable of electroinitiating polymerization are postulated. The observed losses in solution conductivities during polymerization with the quaternary phosphonium and arsonium electrolytes indicate possible interaction between the initiating radical-ionic species and the supporting electrolyte. In an attempt to further elucidate the mechanism of initiation in these systems, a separate series of experiments, employing the nonpolymerizing monomer, 1,1-diphenylethylene, has been carried out.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 15 (1977), S. 2673-2684 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The zinc chloride-catalyzed polymerization of 2-vinylnaphthalene (VN) with both photoinitiation and electronitiation methods was examined. Good yields were obtained with both methods, the electroinitiated process being somewhat faster. The mechanism for polymerization initiation was investigated through a detailed comparison of the kinetics. Both initiation methods show a similar response to increasing input energy and to change in salt to monomer mole ratio. Both methods indicate formation of a ZnCl2-(2-VN)2 complex as intermediate with the formation of the species being rate-determining. These results, together with other similar investigations, are then used to deduce a mechanism that involves the formation of an electronically excited donor-acceptor complex. It is argued that in certain salt-stabilized, electron-delocalized, aromatic systems, such excitation is possible in electroinitiation.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 17 (1979), S. 1411-1418 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The electroinitiated polymerizations of styrene, 2-vinylnaphthalene, and 9-vinylanthracene were compared in sulfolane and acetone solvents in the presence of ZnCl2. The relative orders of polymerization rates and polymerization efficiencies, in both solvents, were 9-vinylanthracene 〉 2-vinylnaphthalene 〉 styrene, with faster rates and higher efficiencies occurring in sulfolane. Data obtained from viscosity and gel permeation chromatography (GPC) studies indicate that the molecular weights of the polymers produced in these systems are extremely low, 〈5000. Chemical composition and infrared (IR) spectral data suggest that abnormal transfer reactions (possibly from solvent) may be occurring in the electroinitiated 9-vinylanthracene polymerizations. The polymerization mechanism appears to be cationic in these monomer-solvent systems with ZnCl2.
    Additional Material: 7 Ill.
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